A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522886



Internal ID18821167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:37593912..37999846hg38UCSC Ensembl
Innerchr12:37987714..38393648hg19UCSC Ensembl
Innerchr12:36273981..36679915hg18UCSC Ensembl
Cytoband12q11
Allele length
AssemblyAllele length
hg38405935
hg19405935
hg18405935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047523
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3522886
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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